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Primary carnitine deficiency is a genetic disorder of the cellular carnitine delivery system that typically manifests around the age of five with symptoms of cardiomyopathy, skeletal muscle weakness and hypoglycemia

The incidence of PPT was reduced from 48.6 to 28.6% in the treated group, and the incidence of permanent hypothyroidism was equivalently reduced

Thus, caution should be taken in monitoring for hypoglycemia when adding additional anti-diabetic medication

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Huberman Lab: short-term stress blocks hunger, but stress lasting more than four to seven days flips into hunger specifically for high-fat, high-sugar comfort foods via the glucocorticoid receptor pathway